Anticoags Part 1 Flashcards

1
Q

What mediator cause platelets to aggregate?

A

TXA 2

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2
Q

What is secondary Hemostasis?

A

The formation of a fibrin clot via a intrinsic pathway or extrinsic pathway

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3
Q

Which patients are anticoagulated with warfarin

A

Afib and mechanical heart valves

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4
Q

What are the LMWH drugs

A

Enoxaparin, dalteparin, tinzaparin

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5
Q

What is the med used for heparin OD

A

Protamine sulfate

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6
Q

What forms together to form a clot that patches an injured blood cell?

A

Fibrin and platelet aggregate

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7
Q

What are the three main components of blood clots

A

Platelets, thrombin, and fibrin

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8
Q

What forms TXA2

A

Arachidonic acid and COX

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9
Q

What is the extrinsic pathway

A

Factor VII activated and initiates cascade, it is short than the intrinsic pathway

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10
Q

What factor activates the intrinsic pathway

A

XII

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11
Q

What results in disorders from the coagulation cascade from extrinsic pathway

A

Bleeding into cavities and subcutaneous hematomas

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12
Q

What results from primary hemostasis

A

Mucus bleeding, petechiae

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13
Q

Which disease can result from both pathways?

A

Von willebrand disease

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14
Q

What is the molecule that inhibits the extrinsic pathway

A

Tissue factor pathway inhibitor

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15
Q

What does factor X convert to in the extrinsic pathway

A

Factor II

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16
Q

What is released by the body to dissolute clots

17
Q

What can cause prolonged bleeding after minor trauma

A

Primary platelet plug

18
Q

CHA2DS2 VASc what falls into 1 pt and 2 point?

A

1pt- HF, HTN, and ages 65-74 female
2pts- age > 75 history of stroke, TIA, or thromboembolism

19
Q

What are the direct factor inhibitors

A

Rivaroxaban, apixaban, edoxaban

20
Q

What antibody is formed in HIT in response to heparin

21
Q

What is most important for monitoring of heparin

A

aPTT, and Xa and thrombin

22
Q

What is the therapeutic range of UFH

A

1.5-2.5 ULN

23
Q

T or F does heparin degrade clots